The histamine H4 receptor mediates inflammation and pruritus in Th2-dependent dermal inflammation

J Invest Dermatol. 2010 Apr;130(4):1023-33. doi: 10.1038/jid.2009.358. Epub 2009 Nov 12.

Abstract

The role of histamine H(4) receptor (H(4)R) was investigated in a T-helper type 2 (Th2)-cell-mediated mouse skin inflammation model that mimics several of the features of atopic dermatitis. Treatment with two specific H(4)R antagonists before challenge with FITC led to a significant reduction in ear edema, inflammation, mast cell, and eosinophil infiltration. This was accompanied by a reduction in the levels of several cytokines and chemokines in the ear tissue. Upon ex vivo antigen stimulation of lymph nodes, H(4)R antagonism reduced lymphocyte proliferation and IL-4, IL-5, and IL-17 levels. One explanation for this finding is that lymph nodes from animals dosed with the H(4)R antagonist, JNJ 7777120, contained a lower number of FITC-positive dendritic cells. The effect of H(4)R antagonism on dendritic cell migration in vivo may be an indirect result of the reduction in tissue cytokines and chemokines or a direct effect on chemotaxis. In addition to anti-inflammatory effects, JNJ 7777120 also significantly inhibited the pruritus shown in the model. Therefore, the dual effects of H(4)R antagonists on pruritus and Th2-cell-mediated inflammation point to their therapeutic potential for the treatment of Th2-mediated skin disorders, including atopic dermatitis.

MeSH terms

  • Animals
  • Chemotaxis / drug effects
  • Chemotaxis / immunology
  • Dendritic Cells / cytology
  • Dendritic Cells / immunology
  • Dermatitis, Atopic / drug therapy
  • Dermatitis, Atopic / immunology*
  • Dermatitis, Atopic / physiopathology
  • Disease Models, Animal
  • Edema / drug therapy
  • Edema / immunology
  • Edema / physiopathology
  • Eosinophils / drug effects
  • Eosinophils / immunology
  • Fluorescein-5-isothiocyanate
  • Histamine Antagonists / pharmacology
  • Indoles / pharmacology
  • Interleukin-17 / metabolism
  • Interleukin-4 / metabolism
  • Interleukin-5 / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Mice, Mutant Strains
  • Piperazines / pharmacology
  • Pruritus / drug therapy
  • Pruritus / immunology*
  • Pruritus / physiopathology
  • Receptors, G-Protein-Coupled / antagonists & inhibitors
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / immunology*
  • Receptors, Histamine / genetics
  • Receptors, Histamine / immunology*
  • Receptors, Histamine H4
  • Th2 Cells / cytology
  • Th2 Cells / immunology*
  • Th2 Cells / metabolism

Substances

  • Histamine Antagonists
  • Hrh4 protein, mouse
  • Indoles
  • Interleukin-17
  • Interleukin-5
  • Piperazines
  • Receptors, G-Protein-Coupled
  • Receptors, Histamine
  • Receptors, Histamine H4
  • Interleukin-4
  • 1-((5-chloro-1H-indol-2-yl)carbonyl)-4-methylpiperazine
  • Fluorescein-5-isothiocyanate